#LupusSymptoms - Joint Pain

Preventing the unbearable joint pain caused by lupus is just one reason why we are so committed to funding the world’s most innovative science that can lead to the most promising treatments. In this video, hear how nine lupus warriors describe their joint pain.

Lupus affects millions worldwide, and there is no cure. Please help the Lupus Research Alliance to raise awareness and funds for lupus research.

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[deluzlalman]

God please heal my daughter and thoes people in your name amen.

[sinthiyaislam]

it was too much painful😭, i can't explain how it feels. sometimes people don't even understand what is going through me. I can't go to university. i have to go outside covering myself, I lost my hair. i got rashes 😭😭

[purple_crocheter]

I feel the same way about the limbs cutting off part just in so much pain

[taneshabeverly]

I haven’t been diagnosed yet I was diagnosed with connective tissue disease, but I have the extreme joint pain in my hands, wrist, feet, & and hips sometimes I can’t walk or stand for long periods of time. I’m about to see another doctor next week. I can’t even lift my arms up my hands and my neck aches.

[sinjinmonsoon]

Lupus has got me right now. I also have painful rash on my face and hands.

[Vei_okii]

In a middle of being diagnosed for lupus and I had joint pain 5 months before I got to convinced my mom to a check up.. it started on my arms (shoulders and elbows) and it went down to my right knees had to get an X-ray cuz I had a fall but it was all clear.. knew that something was off until both of my knees starts to swell.. and then my fingers a few weeks after it attacked my fingers one by one.. and until I got a blood test positive for lupus :<< something died in me that day I stopped drawing and it stopped me from doing alot of activities in school, hate to see my little sister have to take care of me willingly.. she helps me with opening doors bottles ect… hope someone can find a cure for lupus 😞

[nicolemarie]

I was just diagnosed... took 3months!
My life is a lot different now and I’m constantly in pain or uncomfortable! I’m an ex opioid addict and have been clean for 7yrs. So pain medicine is Not an option. Ibuprofen helped but they took me off of it because my kidneys are being effected by the Lupus and it’s causing high blood pressure. Been up ALL night because of my knees and hips 😩😢
Lord help me! 🤍🙏✝️

[arrowb]

Oh, too bad. This video only last 1:21 and FAR TOO SHORT for me to watch. Great to have SLE community to speak of their pains. Feel sad my mum had this life long disease and currently I got funny acte joint pains esp finger and toes. Now I need to differentiate this pains from the SLE from the others. I got negative blood screen test for SLE before symptoms shown, now I got 7/10 of my finger pains in COVID isolation time. Wondering what went wrong with my body and my another new life

[krystahnash]

I'm having a horrible flare up right now. My hands are so swollen that I can't even make a closed fist.

[ENEMA_AND_YOGA_CHANNEL]

I also use coffee enemas for joint pain.

[roxygonzalez]

Am sorry everyone am going through this right now I didn't know what was wrong with me until today my doctor give me the results of some blood work I keep on falling I just couldn't handle my leg my hands now affecting my neck

[fuzzylogics]

is it also like it can come up instantly and be very severe, like one day it may feel like an airbag POOF goes off in a joint and pain ensues directly and a day later it may be gone completely then two days later it's your index finger or some other weird place. Like just now from one moment to the next I lifted my leg off the couch and PFOOF I'm cripple, my knee feels swollen as heck but you can't see it on the outside but I'm limping from pain. Just two days ago it was my right wrist.
I was discussing this with my dad only two weeks ago and describing how crazy fast the pain explodes but also can vanish as quickly as it came and my dad interrupted me with "and you feel like a crazy person because you know if you contact the family doctor the pain will be gone probably before you can get an appointment? Yeah. You got that from me. " And he was never diagnosed. Nor am I. I've been looking online for what it could be and this actually is the first time I'm like: woah. That sounds like me!
I feel like what my mom told me as a kid when I was trying to stay home/ not go to school and was looking for excuses she said "Yeah-yeah and when I press my toe the tip of my nose hurts, right??" like that made up thing she always talked about is now ACTUALLY happening to me? Well, almost. It FEELS like I would be saying something ridiculous, so I hardly tell people and I don't really feel like visiting the doctor..

[janethnunez]

Help
I’m suffering from extreme joint pain. I have been to so many doctors and specialists and chiropractors and everyone says I’m fine. But there are days where I literally feel like my body me mine, my joints get so flared up and I can’t take it. There was a period after pregnancy where it was every single day. It affected my ability to drive and even hold a pencil or spoon. There’s days I can’t even give myself water because I have no strength in my hands. Now the pain comes and goes in different areas but when it hits my whole body I seriously feel like I can’t move. Even blankets hurt my toes.
I’m only 24 and have been living with joint pain since middle school. But no one tells me anything 😭

[khy]

Anyone having issues with their ankles? I can barely walk on my left ankle, 2 complete hip replacements and now this. I don’t know if it’s an ankle replacement but I don’t want it.

[SunflowerJuliet]

wherever i have blood in my body, i have everywhere

[DASNI]

bro yall i got diagnosed w lupus nd i have joint pain and my knees nd ankles hurt so bad i cant sleep at night yall help 😔🙏🙏

[nidzaperez]

I have lupus. Im 60. My ears. Get hard head sours. Yes. All this. 😔😔😔